Literature DB >> 18941710

Unusual glomerulopathy with aggregated subepithelial microspheric particles resembling membranous nephropathy: a variant of glomerulopathy associated with podocytic infolding?

Shinsuke Nomura1, Michiyo Inoue-Kiyohara, Kazuki Oosugi, Eiji Ishikawa, Toshihide Obe, Terumi Horiki, Masaaki Ito.   

Abstract

A 69-year-old woman presented with unusual electron microscopic findings. The patient was admitted to ascertain the cause of her persistent proteinuria, and kidney biopsy was performed. While light microscopic findings and immunofluorescence study suggested membranous nephropathy, electron microscopic study showed microspheric particles aggregated in the subepithelial space where electron-dense deposits should have existed. While the microspheric particles could have been unusual and rough deposits, detailed study suggested that the particles could be parts of glomerular podocytes, for example foot processes. This unusual finding was considered as being in a unique clinical course of membranous nephropathy, but a variant of glomerulopathy associated with podocytic infolding, proposed by Joh et al. (J Nephrol 49:61-67, 2007), could not be excluded.

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Year:  2008        PMID: 18941710     DOI: 10.1007/s10157-008-0089-7

Source DB:  PubMed          Journal:  Clin Exp Nephrol        ISSN: 1342-1751            Impact factor:   2.801


  6 in total

1.  Antenatal membranous glomerulonephritis due to anti-neutral endopeptidase antibodies.

Authors:  Hanna Debiec; Vincent Guigonis; Béatrice Mougenot; Fabrice Decobert; Jean-Philippe Haymann; Albert Bensman; Georges Deschênes; Pierre M Ronco
Journal:  N Engl J Med       Date:  2002-06-27       Impact factor: 91.245

2.  [A preliminary report of national research on podocytic infolding glomerulopathy].

Authors:  Kensuke Joh; Takashi Taguchi; Yutaka Kobayashi; Hiroshi Sato; Shinichi Nishi; Ritsuko Katafuchi; Shinsuke Nomura; Hirofumi Makino; Takao Saito; Hidekazu Shigematsu
Journal:  Nihon Jinzo Gakkai Shi       Date:  2007

3.  Extracellular clusters of spherical microparticles in glomeruli in human renal glomerular diseases.

Authors:  P M Burkholder; L R Hyman; T A Barber
Journal:  Lab Invest       Date:  1973-04       Impact factor: 5.662

4.  Hereditary chronic nephritis (alport) complicated by nephrotic syndrome. Light, Fluorescent and electronmicroscopic studies of renal biopsy specimens.

Authors:  Y Kinoshita; G Osawa; T Morita; N Kobayashi; J Wada
Journal:  Acta Med Biol (Niigata)       Date:  1969-09

5.  A splicing mutation in the alpha 5(IV) collagen gene of a family with Alport's syndrome.

Authors:  S Nomura; G Osawa; T Sai; T Harano; K Harano
Journal:  Kidney Int       Date:  1993-05       Impact factor: 10.612

6.  Distribution of basement membrane antigens in glomeruli of mice with autoimmune glomerulonephritis.

Authors:  S Matsuo; J R Brentjens; G Andres; J M Foidart; G R Martin; A Martinez-Hernandez
Journal:  Am J Pathol       Date:  1986-01       Impact factor: 4.307

  6 in total
  2 in total

1.  Proposal of podocytic infolding glomerulopathy as a new disease entity: a review of 25 cases from nationwide research in Japan.

Authors:  Kensuke Joh; Takashi Taguchi; Hidekazu Shigematsu; Yutaka Kobayashi; Hiroshi Sato; Shinichi Nishi; Ritsuko Katafuchi; Shinsuke Nomura; Yoshihide Fujigaki; Yasunori Utsunomiya; Hitoshi Sugiyama; Takao Saito; Hirofumi Makino
Journal:  Clin Exp Nephrol       Date:  2008-11-18       Impact factor: 2.801

2.  Podocytic infolding in Schimke immuno-osseous dysplasia with novel SMARCAL1 mutations: a case report.

Authors:  Shiqiu Xiong; Lanjun Shuai; Xiaoyan Li; Xiqiang Dang; Xiaochuan Wu; Qingnan He
Journal:  BMC Nephrol       Date:  2020-05-11       Impact factor: 2.388

  2 in total

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